Gas Exchange Flashcards
1
Q
What is CF?
A
- inherited autosomal recessive disorder of exocrine glands due to genetic mutation
- defected gene affects chloride-ion transport across the exocrine and epithelial cells resulting in thick, viscous mucus production
- mucus accumulates, dilates, precipitates, coagulates to form concretions in glands and ducts
2
Q
How is CF tested for?
A
- Sweat testing is the gold standard. If more than 60 millimoles per ml indicates high likelihood of CF
3
Q
Respiratory Manifestations of CF
A
- Stagnation of mucus and bacterial colonization results in destruction of lung tissue
- bacteria colonized in lungs at all times, normal peeps have sterile lungs
- tenancies secretions difficult to expectorate and obstruct the bronchi
4
Q
CF Medications
A
- Pulmozyme (Dornase Alfa)
- Mucomyst (Acetylcysteine)
- TOBI (Tobramycin inhalation solution
- Oral antibiotics
- Quinolones
- IV antibiotics
5
Q
What is Pulmozyne (Dornase Alfa)?
A
- 1st CF-specific drug approved
- MOA: enzyme produced by recombinant gene technology selectively cleaves DNA, thus reducing mucous viscosity and improving airflow (super expensive 7k a month)
6
Q
What is Mucomyst?
A
- inhaled solution (bronchodilator before given) that helps thin and loosen mucus to make it easier to breath
- side effects: bronchial irritation, increased inflammation mucus, bronchospasm
7
Q
What is TOBI?
A
- tobramycin inhalation solution
- treat initial p aeuruginosa infections, acute infections and suppress chronic infections
- benefits: improve lung function, reduce exacerbations, reduce hospitalizations, reduce need for IV antibiotics and improve QOL
8
Q
Asthma risk factors
A
Low birth rate, family history of asthma or allergies
9
Q
Pneumonia
A
inflammation of lung parenchyma, 8th leading cause of infectious disease
10
Q
Causes of pneumonia
A
Aspiration, inhalation, bacteria, fungi, viruses
11
Q
Pneumonia CF
A
- cough - pleuritic chest pain
- fever
- shaking/chills
- rhonchi/crackles
12
Q
Complications of pneumonia
A
- Pleuritis
- pleural effusion
- empyema (alveoli lose elasticity)
- atelectasis (collapsing)
13
Q
meds for pneumonia
A
antibiotics therapy, immunizations
14
Q
pneumonia nursing interventions
A
- Increase oral fluid intake
- incentive spirometry
- endotracheal suctioning
- oxygen therapy
- chest physiotherapy
15
Q
Lung Development in Premature Infants
A
- Alveoli are rarely present and functional prior to 36 weeks
- smaller respiratory lumen, immature capillaries, deficient surfactant results in poor ventilation and gas exchange
- the best ventilators still rely on your body to be able to exchange gas